RIGHT REMEDIES IMMEDIATE RELEASE Mucus Relief DM

Manufacturer
Strive Pharmaceuticals Inc.
Effective date
2026-07-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-08-07 01:01:03

Label at a glance#

ProductRIGHT REMEDIES Mucus Relief DM
Active ingredientDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
Label structure10 sections

Indications and uses

• helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive •  temporarily relieves:    • cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants    • the intensity of coughing  • the impulse to cough to help you get to sleep

Dosage and administration

•  do not exceed 6 tablets in 24 hours, unless directed by a doctor adults and children 12 years of age and over take 1 tablet every 4 hours with a full glass of water while symptoms persist c​hildren under 12 years of age do not use

Storage and handling

• store at 20-25°C (68-77°F) • keep bottle tightly closed • protect from light, heat and moisture

Label contents#

Full prescribing information#

Active ingredients (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Dextromethorphan HBr 20 mg
Guaifenesin 400 mg

Purposes

OTC - PURPOSE SECTION

Cough suppressant
Expectorant

Uses

INDICATIONS & USAGE SECTION

• helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
• temporarily relieves:
   • cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants
   • the intensity of coughing • the impulse to cough to help you get to sleep

Warnings

WARNINGS SECTION

Do not use • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have
• cough accompanied by too much phlegm (mucus)
• persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema

When using this product • do not use more than directed

Stop use and ask a doctor if cough lasts more than 7 days, recurs, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

If pregnant or breast-feeding, ask a health care professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.

Directions

DOSAGE & ADMINISTRATION SECTION

• do not exceed 6 tablets in 24 hours, unless directed by a doctor

adults and children 12 years of age and overtake 1 tablet every 4 hours with a full glass of water while symptoms persist
c​hildren under 12 years of agedo not use

Other information

STORAGE AND HANDLING SECTION

• store at 20-25°C (68-77°F) • keep bottle tightly closed
• protect from light, heat and moisture

Inactive ingredients

INACTIVE INGREDIENT SECTION

colloidal silicon dioxide, hydroxypropyl methylcellulose, magnesium stearate, maltodextrin, microcrystalline cellulose, polyethylene glycol, polyvinyl pyrrolidone, sodium starch glycolate, stearic acid

Questions or comments?

OTC - QUESTIONS SECTION

1 (888) 577-8033 Monday-Friday 8am-4pm EST

SPL UNCLASSIFIED SECTION

IMMEDIATE RELEASE

• Controls cough,
• Thins & loosens mucus

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

Distributed by:
Strive Pharmaceuticals Inc.,
East Brunswick, NJ 08816
PRODUCT OF INDIA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RR Mucus Relief DMRR Mucus Relief DM

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130370692001334GTIN-13: 0370692001334
EAN-13: 0370692001334
GTIN-12: 370692001334
UPC-A: 370692001334
GTIN storage (14 digits): 00370692001334
70692181-3.jpg
BarcodeEAN-130370692001341GTIN-13: 0370692001341
EAN-13: 0370692001341
GTIN-12: 370692001341
UPC-A: 370692001341
GTIN storage (14 digits): 00370692001341
70692181-3.jpg
QR code linkQR Coderightremedies.com/70692181-3.jpg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70692-18170692-181-81, 70692-181-25

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-06-01full-release2026-06-05 00:30:39

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RIGHT REMEDIES Mucus Relief DMDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESINStrive Pharmaceuticals Inc.51c4dcfb-8725-d547-e063-6394a90ac04c2026-07-31WarningsExact identifier
ndc (package): 70692-181-81
ndc (package): 70692-181-25
ndc (product): 70692-181
ndc11 (package): 70692018125
ndc11 (package): 70692018181
spl id: 1a32121b-7987-4333-8225-bf057edde204
spl set id: 51c4dcfb-8725-d547-e063-6394a90ac04c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.